Idiopathic myointimal hyperplasia of the mesenteric veins-a report of two cases.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
AME Case Reports Pub Date : 2024-08-09 eCollection Date: 2024-01-01 DOI:10.21037/acr-23-59
Martin Uwah, Leonardo Bustamante-Lopez, Liam Devane, John Hoff, Norbert Garcia-Henriquez, Brian Kline, John R T Monson, Matthew Albert
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Abstract

Background: Idiopathic myointimal hyperplasia of the mesenteric veins (IMHMV) is a rare condition that poses a diagnostic challenge to surgeons and pathologists alike. Our aim is to describe two cases of IMHMV requiring operative intervention. The challenge going forward is accurately and systematically identifying factors from both a pathologic and clinical perspective that guide timely diagnosis and avoid unnecessary treatment.

Case description: A 37-year-old male with no significant past medical history was evaluated for a two-month history of abdominal pain, constipation, diarrhea and recent bleeding per rectum. Computed tomography (CT) scan revealed abnormal wall thickening with surrounding inflammatory changes and mesenteric edema involving the descending and sigmoid colon as well as the rectum. The patient was taken to the operating room where he underwent a laparoscopic-assisted extended left colectomy with end colostomy. The patient did well postoperatively and was ultimately meeting all goals for discharge by postoperative day 9. A 49-year-old male with a past medical history of hypertension, gastroesophageal reflux and recent coronavirus disease 2019 (COVID-19) infection was admitted to another hospital following several months of colitis of unknown etiology; unresponsive to antibiotics and steroids. CT scan revealed concentric, severe mural thickening and intramural edema of the distal descending colon extending to the rectum consistent with proctocolitis. The patient was taken to the operating room where he underwent a laparoscopic-assisted low anterior resection with end colostomy with findings of an extremely indurated, thickened left colon and rectum. The patient recovered from these additional interventions and was discharged home in stable condition on postoperative day 32.

Conclusions: A multidisciplinary team approach to this condition will be vital to administering the appropriate treatment modalities for future cases of IMHMV.

肠系膜静脉特发性肌内膜增生症--两例病例的报告。
背景:肠系膜静脉特发性肌内膜增生症(IMHMV)是一种罕见病,给外科医生和病理学家的诊断都带来了挑战。我们的目的是描述两例需要手术干预的 IMHMV 病例。未来的挑战在于从病理学和临床角度准确、系统地识别各种因素,从而指导及时诊断,避免不必要的治疗:一名 37 岁男性,既往无重大病史,因腹痛、便秘、腹泻和近期直肠周围出血两个月病史接受评估。计算机断层扫描(CT)显示降结肠、乙状结肠和直肠壁异常增厚,周围有炎症变化和肠系膜水肿。患者被送入手术室,在腹腔镜辅助下接受了扩大左结肠切除术和结肠造口术。患者术后表现良好,最终在术后第 9 天达到了出院的所有目标。一名 49 岁的男性患者既往有高血压、胃食管反流病史,近期曾感染 2019 年冠状病毒病(COVID-19),在出现病因不明的结肠炎数月后住进了另一家医院;患者对抗生素和类固醇无反应。CT 扫描显示降结肠远端有同心圆状、严重的壁层增厚和壁层内水肿,并延伸至直肠,与直肠结肠炎一致。患者被送进手术室,在腹腔镜辅助下接受了低位前切除术和结肠造口术,术中发现左侧结肠和直肠极度硬化、增厚。患者从这些额外的干预中恢复过来,术后第 32 天病情稳定出院回家:结论:多学科团队对这种病症的处理方法对今后的 IMHMV 病例采取适当的治疗方式至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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